A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7112



Internal ID15552089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:137528973..137563593hg38UCSC Ensembl
OuterchrX:136611132..136645752hg19UCSC Ensembl
OuterchrX:136438798..136473418hg18UCSC Ensembl
OuterchrX:136336652..136371272hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg385404
hg195404
hg185404
hg175404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2841
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7112
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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